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Updated: Jul 27, 2025

Using Scaffold Liposomes to Reconstitute Lipid-proximal Protein-protein Interactions In Vitro
Published on: January 11, 2017
Different tether proteins of the same membrane contact site affect the localization and mobility of each other
Lucia Amado1, Alexandra P Cogan1, Ayelén González Montoro1,2
1Department of Biology/Chemistry, Cellular Communication Laboratory, Osnabrück University, Barbarastraße 13, D-49076 Osnabrück, Germany.
Abstract:
Membrane contact sites enable the exchange of metabolites between subcellular compartments and regulate organelle dynamics and positioning. These structures often contain multiple proteins that tether the membranes, establishing the apposition and functionalizing the structure. In this work, we used drug-inducible tethers in vivo in Saccharomyces cerevisiae to address how different tethers influence each other. We found that the establishment of a region of membrane proximity can recruit tethers, influencing their distribution between different locations or protein complexes. In addition, restricting the localization of one tether to a subdomain of an organelle caused other tethers to be restricted there. Finally, we show that the mobility of contact site tethers can also be influenced by other tethers of the same interface. Overall, our results show that the presence of other tethers at contact sites is an important determinant of the behavior of tethering proteins. This suggests that contact sites with multiple tethers are controlled by the interplay between specific molecular interactions and the cross-influence of tethers of the same interface.
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